| 8 April 2019 | Trisomy 21 is a Cause of Permanent Neonatal Diabetes that is Autoimmune but not HLA Associated | Johnson, MBJ; De Franco, E; Atma W Greeley, S; et al. |
| 4 September 2019 | GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI | Alves, AC; De Silva, NMG; Karhunen, V; et al. |
| 16 January 2013 | Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency | De Franco, E; Shaw-Smith, C; Flanagan, SE; et al. |
| 6 December 2012 | GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiency | De Franco, E; Shaw-Smith, C; Flanagan, SE; et al. |
| 20 August 2019 | Clusters provide a better holistic view of type 2 diabetes than simple clinical features – Authors' reply | Dennis, JM; Shields, BM; Henley, WE; et al. |
| 27 November 2018 | Future Roadmaps for Precision Medicine Applied to Diabetes: Rising to the Challenge of Heterogeneity | Bowman, P; Flanagan, SE; Hattersley, AT |
| 18 December 2019 | Patterns of postmeal insulin secretion in individuals with sulfonylurea-treated KCNJ11 neonatal diabetes show predominance of non-K ATP -channel pathways | Bowman, P; McDonald, TJ; Knight, BA; et al. |
| 8 November 2019 | Absence of islet autoantibodies and modestly raised glucose values at diabetes diagnosis should lead to testing for MODY: Lessons from a 5-year pediatric Swedish national cohort study | Carlsson, A; Shepherd, M; Ellard, S; et al. |
| 18 November 2010 | Integrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locus | Bell, CG; Finer, S; Lindgren, CM; et al. |
| 18 June 2019 | Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis | Thompson, WD; Tyrrell, J; Borges, MC; et al. |
